Telomelysin shows potent antitumor activity through apoptotic and non-apoptotic cell death in soft tissue sarcoma cells

被引:4
|
作者
Li, Gui-Dong [1 ,2 ]
Kawashima, Hiroyuki [1 ]
Ogose, Akira [1 ]
Ariizumi, Takashi [1 ]
Hotta, Tetsuo [1 ]
Kuwano, Ryozo [3 ]
Urata, Yasuo [4 ]
Fujiwara, Toshiyoshi [5 ,6 ]
Endo, Naoto [1 ]
机构
[1] Niigata Univ, Grad Sch Med & Dent Sci, Div Orthoped Surg, Niigata, Japan
[2] Harbin Med Univ, Affiliated Hosp 2, Dept Orthoped Surg, Harbin, Peoples R China
[3] Niigata Univ, Brain Res Inst, Ctr Bioresource Based Res, Dept Mol Genet & Bioinformat, Niigata, Japan
[4] Oncolys BioPharma Inc, Tokyo, Japan
[5] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Surg, Div Surg Oncol, Okayama 7008530, Japan
[6] Okayama Univ Hosp, Ctr Gene & Cell Therapy, Okayama, Japan
来源
CANCER SCIENCE | 2013年 / 104卷 / 09期
关键词
REPLICATION-SELECTIVE ADENOVIRUS; CATALYTIC SUBUNIT HTERT; PHASE-II TRIAL; CANCER-CELLS; IN-VIVO; AUTOPHAGY; INHIBITION; NECROSIS; RECEPTOR; TUMORS;
D O I
10.1111/cas.12208
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This study investigated the pathway underlying the antitumor activity of telomelysin, a telomerase-dependent, replication-selective oncolytic adenovirus, in soft tissue sarcoma cells. Treatment with telomelysin alone resulted in simultaneous induction of apoptosis and autophagy, whereas cotreatment with telomelysin and 3-methyladenine significantly reduced cell viability and increased apoptosis and the cellular ATP level compared to treatment with telomelysin alone, indicating that telomelysin-mediated autophagy is a death-protective but not death-promoting process. Cotreatment with Z-Val-Ala-Asp-CH2F significantly increased cellular ATP depletion compared to telomelysin-alone treatment while inhibiting telomelysin-induced apoptosis and having no significant effect on cell viability, indicating that it promotes transition from apoptotic to necrotic cell death.
引用
收藏
页码:1178 / 1188
页数:11
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